EP0424545A1 - Method for preparing alcoholic beverages - Google Patents

Method for preparing alcoholic beverages Download PDF

Info

Publication number
EP0424545A1
EP0424545A1 EP90907420A EP90907420A EP0424545A1 EP 0424545 A1 EP0424545 A1 EP 0424545A1 EP 90907420 A EP90907420 A EP 90907420A EP 90907420 A EP90907420 A EP 90907420A EP 0424545 A1 EP0424545 A1 EP 0424545A1
Authority
EP
European Patent Office
Prior art keywords
heating
diacetyl
fermentation liquor
fermentation
liquor
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP90907420A
Other languages
German (de)
French (fr)
Other versions
EP0424545B1 (en
EP0424545A4 (en
Inventor
Hiroshi Kirin Beer Kabushiki Kaisha Murayama
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kirin Brewery Co Ltd
Original Assignee
Kirin Brewery Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=14804429&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0424545(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Kirin Brewery Co Ltd filed Critical Kirin Brewery Co Ltd
Publication of EP0424545A1 publication Critical patent/EP0424545A1/en
Publication of EP0424545A4 publication Critical patent/EP0424545A4/en
Application granted granted Critical
Publication of EP0424545B1 publication Critical patent/EP0424545B1/en
Anticipated expiration legal-status Critical
Revoked legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12GWINE; PREPARATION THEREOF; ALCOHOLIC BEVERAGES; PREPARATION OF ALCOHOLIC BEVERAGES NOT PROVIDED FOR IN SUBCLASSES C12C OR C12H
    • C12G3/00Preparation of other alcoholic beverages
    • C12G3/02Preparation of other alcoholic beverages by fermentation
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12CBEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00Fermentation processes for beer

Definitions

  • the present invention relates to a process for preparing alcoholic beverages comprising a step of heating a main fermentation liquor, and more particularly, to a process for preparing alcoholic beverages wherein diacetyl precursors contained in the main fermentation liquor are heated and the amount of the diacetyl and its precursors is thus reduced within a short period of time.
  • the process for producing alcoholic beverages comprises a step of the main fermentation in which a microorganism, particularly yeast, is added to a fermentation stock liquor which is an aqueous solution containing a substrate for the microorganism so that the fermentation proceeds together with the proliferation of the microorganism, and a step of the post fermentation which is conducted at a relatively low temperature and in which the fermentation proceeds without the proliferation of the microorganism.
  • a microorganism particularly yeast
  • a fermentation stock liquor which is an aqueous solution containing a substrate for the microorganism so that the fermentation proceeds together with the proliferation of the microorganism
  • a step of the post fermentation which is conducted at a relatively low temperature and in which the fermentation proceeds without the proliferation of the microorganism.
  • One of the principal objects of the post fermentation includes the consumption of the diacetyl compound, which will herein include collectively the diacetyl itself (vicinal diketone) and diacetyl precursors (acetohydroxy acid), which is produced irreversibly as
  • the diacetyl compound produced in the main fermentation is, however, almost present as the diacetyl precursors in the fermentation liquor.
  • yeast can decompose the diacetyl into odorless acetoin which is further converted into 2,3-butanediol, but it cannot decompose the diacetyl precursors.
  • the reaction for converting the diacetyl precursors into the diacetyl is a non-biological and pure chemical reaction. Therefore, the conventional post fermentation carried out at a relatively low temperature has a problem in that the diacetyl precursors are converted into diacetyl only at a low conversion rate, so that it takes a long period of time before the disappearance of the diacetyl compound.
  • the present invention has been achieved on the observation that the conversion of the diacetyl precursors into the diacetyl by heating a fermentation liquor under a predetermined condition brings about not only the decrease of the diacetyl precursor but also the decrease of the diacetyl whereby the amount of the diacetyl compound remarkably decreases when compared with the amount before heating.
  • the object of the present invention is to provide a process for producing alcoholic beverages in which the amount of the diacetyl compound contained in the fermentation liquor is reduced, within a short period of time.
  • the process for producing alcoholic beverages according to the present invention comprises a step of heating a fermentation liquor which has been prepared by subjecting an aqueous solution of a substrate for a microorganism to fermentation which accompanies the proliferation of the microorganism under a condition that a concentration of oxygen dissolved therein of less than 1 mg/lit. is maintained thereby to reduce the quantity in the fermentation liquor of the total of diacetyl and the diacetyl precursors below the level before the heating.
  • the amount of the diacetyl compound as one of the components which are contained in a fermentation liquor and give an unpleasant unmatured smell to alcoholic beverages is reduced appreciably by heating the fermentation liquor which has undergone main fermentation under the condition of a concentration of oxygen dissolved therein of less than 1 mg/lit. being maintained.
  • the conventional process required for the disappearance of the diacetyl compound, that is, the post fermentation step, is not required, or alternatively, even if post fermentation is required, the diacetyl precursor in the fermentation liquor has been previously converted into the diacetyl and the diacetyl remains only in a very small amount, so that the diacetyl compound disappears in a very short time by the contact with yeast and therefore the period required for producing the alcoholic beverages can be substantially shortened.
  • Fig. 1 illustrates a relationship between the heating temperature T and the rate constant K for converting the diacetyl precursor into the diacetyl
  • Fig. 2 illustrates the relationship between the rate constant K for converting the diacetyl precursor into the diacetyl and the period of heating T required for obtaining the amount of the diacetyl conversion V2 (mg/lit.) after the heating
  • Fig. 3 is a diagram which illustrates a typical heating apparatus used in the present invention
  • Fig. 4 illustrates a relationship between the concentration of dissolved oxygen and the decreasing rate of the diacetyl
  • Fig. 5 illustrates a relationship between the period of heating and the decreasing rate of the diacetyl.
  • the fermentation liquor as the object of the present invention is a fermentation liquor which has undergone a main fermentation such that a microorganism, particularly yeast, is added to a fermentation stock liquor as a substrate for the microorganism so that the fermentation proceeds together with the proliferation of the microorganism.
  • the substrate for microorganisms is generally sugar, and is wort (which may have hops added) when the alcoholic drink to be produced is beer, and is obtained by saccharification of starches of barley and/or wheat with an enzyme of the malt thereof, and is a fruit juice when the alcoholic beverage to be produced is wine, particularly a grape juice.
  • a typical microorganism for the alcoholic fermentation of such a substrate is yeast.
  • the typical beer yeast is the one of Saccharomyces , for example, Saccharomyces cerevisiae .
  • the concentration of the microorganism in the fermentation liquor is preferably 106 cells/ml or less. Higher microorganism concentration than 106 cells/ml, is not preferable since the microorganism components are transferred into the fermentation liquor by heating.
  • the heating of the fermentation liquor of the present invention requires the condition that the dissolved oxygen concentration be maintained at a level lower than 1 mg/lit. If the dissolved oxygen concentration is in the range of 1 mg/lit. or more, the amount of the diacetyl precursors contained as the precursor in the fermentation liquor will not be reduced in a short time, and no advantages inherent in the present invention will not be attained.
  • the means for establishing and maintaining the dissolved oxygen concentration at a level of less than 1 mg/lit. of the fermentation liquor is not especially limited. Generally, the fermentation liquor in which the main fermentation has been completed is in an anaerobic state (generally in 0.1 mg/lit.
  • the dissolved oxygen concentration is preferably in the range of 0.2 mg/lit. or less, more preferably substantially zero.
  • the dissolved oxygen concentration in the fermentation liquor is determined by a conventional dissolved oxygen meter such as Model 58 manufactured by Yellow Springs Instrument Co., Inc. Yellow Springs, Ohio, U.S.A.
  • Heating of the fermentation liquor is conducted under the conditions of a temperature and a duration of time sufficient enough for reducing the concentration of the total of diacetyl and the diacetyl precursors to a level significantly lower than that before the heating.
  • the heating temperature of the fermentation liquor is appropriately determined in the range of 40 to 120°C. Heating at a temperature lower than 40°C will cause the problem that the renewed production of the diacetyl precursor or the fermentation are promoted. Heating at a temperature higher than 120°C will cause the problem that insoluble proteinous products generated by heat will impair the quality of the alcoholic beverage produced.
  • the minimum requisite heating time at the heating temperature determined from the aforementioned temperature range can be determined corresponding to the amount of the diacetyl precursor in the fermentation liquor. That is to say, the relationship (correlation-1) between the heating temperature T in the heating temperature range of 40 to 120°C and the rate constant for converting the diacetyl precursor into the diacetyl is obtained (Fig. 1).
  • the combination (V1, V2) of the content, V1 (mg/lit.), of the diacetyl precursor in the fermentation liquor before heating and the objective or desired value, V2 (mg/lit.), of the residual amount of the diacetyl precursor after heating are determined.
  • the combination (V1, V2) is determined as shown in (i) or (ii) below:
  • the relationship (correlation-2) between the rate constant K of conversion and the heating time t for obtaining the objective value V2 (mg/lit.) of the residual amount of the diacetyl precursor after heating is determined (Fig. 2). From these relationships, when the heating temperature T is determined at a level within the range of 40 to 120°C, the rate constant K of conversion corresponding to the heating temperature T is then obtained from the correlation-1 (Fig.
  • the requisite minimal heating time t is determined within the range of 0.003 to 100 hours.
  • the conversion reaction of the diacetyl precursor into diacetyl is of the first order, so that the rate constant K for conversion of the diacetyl precursor into diacetyl can be obtained by dividing, by the predetermined heating time, the natural logarithm of the value obtained by dividing the amount of the diacetyl precursor before heating by the amount of the diacetyl precursor after heating at the predetermined temperature as shown in the following equation:
  • the pressure on the heating of the fermentation liquor may be any pressures so that foaming by carbon dioxide gas of the fermentation liquor will not take place during heating, or the heating may also be carried out without pressurizing. In the case of the heating without pressurizing, the heating efficiency decreases due to the foaming by the carbon dioxide gas, but the effect of the present invention will not be varied.
  • the heating is carried out with any apparatuses which can heat the whole fermentation liquor at a predetermined temperature for a predetermined time.
  • the heating apparatus may be specifically the one based on the principle of a heat exchanger.
  • the heating of the fermentation liquor was conducted with an apparatus illustrated in Fig. 3.
  • the fermentation liquor in the main fermentation tank 1 in which the dissolved oxygen concentration is maintained at a level of less than 1 mg/lit. while carbon dioxide gas is introduced into the main fermentation tank 1 is pumped through the pre-heating apparatus 2 into the heating apparatus 3.
  • the fermentation liquor is subjected to heating treatment at a predetermined temperature for a predetermined time, then cooled through the cooling apparatus 4, and taken out through the pressure controlling valve 5.
  • the content in the fermentation liquor of the diacetyl precursor was determined to be 0.5 mg/lit., and at the heating temperature of 70°C and at the aimed residual amount of the diacetyl precursor after heating of 0.08 mg/lit, the requisite minimal heating time obtained from Figs. 1 and 2 was about 13 minutes.
  • heating was conducted without pressurizing for 40 minutes at the temperatures of 70°C and 80°C, respectively, and then cooling conducted whereby samples (Sample 1 and 2) were obtained.
  • the content of the diacetyl precursor in the fermentation liquor before heating which was 0.5 mg/lit. was reduced to 0.1 mg/lit. after heating at 70°C (Sample 1) and to 0.07 mg/lit. after heating at 80°C (Sample 2).
  • the requisite minimal heating time (14 minutes) was obtained in the same manner as in Example 1, and heating was conducted at the temperatures of 70°C for 40 minutes under the pressure of 7 kg/cm2 in order to suppress the foaming by carbon dioxide gas. Then the cooling of the fermentation liquor gave a sample (Sample 3).
  • the requisite minimal heating times (2 - 42 minutes) were obtained in the same manner as in Example 1, and the fermentation liquor was heated under various heating conditions (temperature, time and pressure) and then cooled to give samples (Samples 4 - 7).
  • the requisite minimal heating time (20 minutes) was obtained in the same manner as in Example 1, and the fermentation liquor was subjected to heating treatment without pressurizing at a heating temperature of 70°C for a heating time of 40 minutes and then cooled to give a sample.
  • the fermentation liquor was subjected to heating treatment for various heating times at three levels of heating temperature (60°C, 70°C and 80°C) and then cooled to give samples.
  • the present invention has a large industrial applicability in view that the present invention can greatly shorten the time for producing alcoholic beverages.

Abstract

A method of producing sake, involving the step of heating fermented liquor, which comprises adjusting the dissolved oxygen concentration of prefermented liquor to less than 1 mg/l and heating the liquor at a given temperature within the range of 40 to 120°C for a time predetermined according to the required target value of the quantity of residual diacetyl precursor. This procedure serves to not only convert most of the diacetyl precursor contained in the prefermented liquor into diacetyl which can easily be decomposed by yeast, but also reduce the quantity of the diacetyl itself. As a result, it now becomes possible to dispense with a prolonged, low-temperature post-fermentation which has hitherto been necessary for reducing the diacetyl content and to greatly shorten the time necessary for producing sake.

Description

    FIELD OF THE ART
  • The present invention relates to a process for preparing alcoholic beverages comprising a step of heating a main fermentation liquor, and more particularly, to a process for preparing alcoholic beverages wherein diacetyl precursors contained in the main fermentation liquor are heated and the amount of the diacetyl and its precursors is thus reduced within a short period of time.
  • BACKGROUND ART
  • The process for producing alcoholic beverages comprises a step of the main fermentation in which a microorganism, particularly yeast, is added to a fermentation stock liquor which is an aqueous solution containing a substrate for the microorganism so that the fermentation proceeds together with the proliferation of the microorganism, and a step of the post fermentation which is conducted at a relatively low temperature and in which the fermentation proceeds without the proliferation of the microorganism. One of the principal objects of the post fermentation includes the consumption of the diacetyl compound, which will herein include collectively the diacetyl itself (vicinal diketone) and diacetyl precursors (acetohydroxy acid), which is produced irreversibly as a metabolite of yeast in the main fermentation thereby to mature the flavor of the alcoholic beverages.
  • The diacetyl compound produced in the main fermentation is, however, almost present as the diacetyl precursors in the fermentation liquor. On the other hand, yeast can decompose the diacetyl into odorless acetoin which is further converted into 2,3-butanediol, but it cannot decompose the diacetyl precursors. Moreover, the reaction for converting the diacetyl precursors into the diacetyl is a non-biological and pure chemical reaction. Therefore, the conventional post fermentation carried out at a relatively low temperature has a problem in that the diacetyl precursors are converted into diacetyl only at a low conversion rate, so that it takes a long period of time before the disappearance of the diacetyl compound.
  • DISCLOSURE OF THE INVENTION
  • The present invention has been achieved on the observation that the conversion of the diacetyl precursors into the diacetyl by heating a fermentation liquor under a predetermined condition brings about not only the decrease of the diacetyl precursor but also the decrease of the diacetyl whereby the amount of the diacetyl compound remarkably decreases when compared with the amount before heating. The object of the present invention is to provide a process for producing alcoholic beverages in which the amount of the diacetyl compound contained in the fermentation liquor is reduced, within a short period of time.
  • The process for producing alcoholic beverages according to the present invention comprises a step of heating a fermentation liquor which has been prepared by subjecting an aqueous solution of a substrate for a microorganism to fermentation which accompanies the proliferation of the microorganism under a condition that a concentration of oxygen dissolved therein of less than 1 mg/lit. is maintained thereby to reduce the quantity in the fermentation liquor of the total of diacetyl and the diacetyl precursors below the level before the heating.
  • According to the present invention, the amount of the diacetyl compound as one of the components which are contained in a fermentation liquor and give an unpleasant unmatured smell to alcoholic beverages is reduced appreciably by heating the fermentation liquor which has undergone main fermentation under the condition of a concentration of oxygen dissolved therein of less than 1 mg/lit. being maintained. The conventional process required for the disappearance of the diacetyl compound, that is, the post fermentation step, is not required, or alternatively, even if post fermentation is required, the diacetyl precursor in the fermentation liquor has been previously converted into the diacetyl and the diacetyl remains only in a very small amount, so that the diacetyl compound disappears in a very short time by the contact with yeast and therefore the period required for producing the alcoholic beverages can be substantially shortened.
  • DESCRIPTION OF THE DRAWINGS
  • Fig. 1 illustrates a relationship between the heating temperature T and the rate constant K for converting the diacetyl precursor into the diacetyl;
    Fig. 2 illustrates the relationship between the rate constant K for converting the diacetyl precursor into the diacetyl and the period of heating T required for obtaining the amount of the diacetyl conversion V2 (mg/lit.) after the heating;
    Fig. 3 is a diagram which illustrates a typical heating apparatus used in the present invention;
    Fig. 4 illustrates a relationship between the concentration of dissolved oxygen and the decreasing rate of the diacetyl; and
    Fig. 5 illustrates a relationship between the period of heating and the decreasing rate of the diacetyl.
  • BEST MODE FOR PRACTICING THE INVENTION
  • The fermentation liquor as the object of the present invention is a fermentation liquor which has undergone a main fermentation such that a microorganism, particularly yeast, is added to a fermentation stock liquor as a substrate for the microorganism so that the fermentation proceeds together with the proliferation of the microorganism.
  • The substrate for microorganisms is generally sugar, and is wort (which may have hops added) when the alcoholic drink to be produced is beer, and is obtained by saccharification of starches of barley and/or wheat with an enzyme of the malt thereof, and is a fruit juice when the alcoholic beverage to be produced is wine, particularly a grape juice.
  • A typical microorganism for the alcoholic fermentation of such a substrate is yeast. The typical beer yeast is the one of Saccharomyces, for example, Saccharomyces cerevisiae.
  • The concentration of the microorganism in the fermentation liquor is preferably 10⁶ cells/ml or less. Higher microorganism concentration than 10⁶ cells/ml, is not preferable since the microorganism components are transferred into the fermentation liquor by heating.
  • The heating of the fermentation liquor of the present invention requires the condition that the dissolved oxygen concentration be maintained at a level lower than 1 mg/lit. If the dissolved oxygen concentration is in the range of 1 mg/lit. or more, the amount of the diacetyl precursors contained as the precursor in the fermentation liquor will not be reduced in a short time, and no advantages inherent in the present invention will not be attained. In this connection, the means for establishing and maintaining the dissolved oxygen concentration at a level of less than 1 mg/lit. of the fermentation liquor is not especially limited. Generally, the fermentation liquor in which the main fermentation has been completed is in an anaerobic state (generally in 0.1 mg/lit. or less) due to the aspiration effect of the yeast, and the aforementioned level of the dissolved oxygen concentration can be maintained by preventing the fermentation liquor from contact with oxygen. The dissolved oxygen concentration is preferably in the range of 0.2 mg/lit. or less, more preferably substantially zero.
  • The dissolved oxygen concentration in the fermentation liquor is determined by a conventional dissolved oxygen meter such as Model 58 manufactured by Yellow Springs Instrument Co., Inc. Yellow Springs, Ohio, U.S.A.
  • Heating of the fermentation liquor is conducted under the conditions of a temperature and a duration of time sufficient enough for reducing the concentration of the total of diacetyl and the diacetyl precursors to a level significantly lower than that before the heating. In view of this, the heating temperature of the fermentation liquor is appropriately determined in the range of 40 to 120°C. Heating at a temperature lower than 40°C will cause the problem that the renewed production of the diacetyl precursor or the fermentation are promoted. Heating at a temperature higher than 120°C will cause the problem that insoluble proteinous products generated by heat will impair the quality of the alcoholic beverage produced.
  • The minimum requisite heating time at the heating temperature determined from the aforementioned temperature range can be determined corresponding to the amount of the diacetyl precursor in the fermentation liquor. That is to say, the relationship (correlation-1) between the heating temperature T in the heating temperature range of 40 to 120°C and the rate constant for converting the diacetyl precursor into the diacetyl is obtained (Fig. 1). Next, the combination (V1, V2) of the content, V1 (mg/lit.), of the diacetyl precursor in the fermentation liquor before heating and the objective or desired value, V2 (mg/lit.), of the residual amount of the diacetyl precursor after heating are determined. For example, the combination (V1, V2) is determined as shown in (i) or (ii) below:
    • (i) V1 = 2.0 mg/lit., V2 = 0.01 mg/lit.;
    • (ii) V1 = 0.2 mg/lit., V2 = 0.08 mg/lit.
  • Then, for the given combination (V1, V2) thus determined, the relationship (correlation-2) between the rate constant K of conversion and the heating time t for obtaining the objective value V2 (mg/lit.) of the residual amount of the diacetyl precursor after heating is determined (Fig. 2). From these relationships, when the heating temperature T is determined at a level within the range of 40 to 120°C, the rate constant K of conversion corresponding to the heating temperature T is then obtained from the correlation-1 (Fig. 1), and the content V1 of the diacetyl precursor in the fermentation liquor before heating is then measured and the objective value V2 of the desired residual amount of the diacetyl precursor after heating is chosen to determine the combination (V1, V2), and the heating time t corresponding to the aforementioned rate constant K of conversion is then determined from the correlation-2 (Fig. 2). The requisite minimal heating time t is determined within the range of 0.003 to 100 hours. In this connection, the conversion reaction of the diacetyl precursor into diacetyl is of the first order, so that the rate constant K for conversion of the diacetyl precursor into diacetyl can be obtained by dividing, by the predetermined heating time, the natural logarithm of the value obtained by dividing the amount of the diacetyl precursor before heating by the amount of the diacetyl precursor after heating at the predetermined temperature as shown in the following equation:
  • K =
    ln (Acetohydroxy acid before heating/Residual acetohydroxy acid)/Predetermined heating time (hr)
  • The pressure on the heating of the fermentation liquor may be any pressures so that foaming by carbon dioxide gas of the fermentation liquor will not take place during heating, or the heating may also be carried out without pressurizing. In the case of the heating without pressurizing, the heating efficiency decreases due to the foaming by the carbon dioxide gas, but the effect of the present invention will not be varied.
  • The heating is carried out with any apparatuses which can heat the whole fermentation liquor at a predetermined temperature for a predetermined time. The heating apparatus may be specifically the one based on the principle of a heat exchanger.
  • EXAMPLES
  • The present invention is further described in detail with reference to the examples of the present invention below.
  • The heating of the fermentation liquor was conducted with an apparatus illustrated in Fig. 3. In Fig. 3, the fermentation liquor in the main fermentation tank 1 in which the dissolved oxygen concentration is maintained at a level of less than 1 mg/lit. while carbon dioxide gas is introduced into the main fermentation tank 1 is pumped through the pre-heating apparatus 2 into the heating apparatus 3. Within the heating apparatus 3, the fermentation liquor is subjected to heating treatment at a predetermined temperature for a predetermined time, then cooled through the cooling apparatus 4, and taken out through the pressure controlling valve 5.
  • Example 1
  • A fermentation liquor which was obtained by the fermentation of wort by a beer yeast, Saccharomyces cerevisiae, namely the main fermentation liquor which had undergone fermentation with proliferation of the yeast taking place, was supplied into a heating apparatus 3 while the fermentation liquor was maintained in an anaerobic state at a dissolved oxygen concentration of 0.1 mg/lit. The content in the fermentation liquor of the diacetyl precursor was determined to be 0.5 mg/lit., and at the heating temperature of 70°C and at the aimed residual amount of the diacetyl precursor after heating of 0.08 mg/lit, the requisite minimal heating time obtained from Figs. 1 and 2 was about 13 minutes. Thus, heating was conducted without pressurizing for 40 minutes at the temperatures of 70°C and 80°C, respectively, and then cooling conducted whereby samples (Sample 1 and 2) were obtained.
  • As shown in Table 1, the content of the diacetyl precursor in the fermentation liquor before heating which was 0.5 mg/lit. was reduced to 0.1 mg/lit. after heating at 70°C (Sample 1) and to 0.07 mg/lit. after heating at 80°C (Sample 2).
    Figure imgb0001
  • Example 2
  • A fermentation liquor which was obtained by the fermentation of a wort by a beer yeast, Saccharomyces cerevisiae, namely the main fermentation liquor, was supplied into a heating apparatus 3 while the fermentation liquor was maintained in an anaerobic state at a dissolved oxygen concentration of 0.1 mg/lit. The requisite minimal heating time (14 minutes) was obtained in the same manner as in Example 1, and heating was conducted at the temperatures of 70°C for 40 minutes under the pressure of 7 kg/cm² in order to suppress the foaming by carbon dioxide gas. Then the cooling of the fermentation liquor gave a sample (Sample 3).
  • As shown in Table 2, the content of the diacetyl precursor in the fermentation liquor before heating which was 0.55 mg/lit. was reduced to 0.13 mg/lit. after heating.
    Figure imgb0002
  • Example 3
  • A fermentation liquor which was obtained by the fermentation of a wort by a beer yeast, Saccharomyces cerevisiae, namely the main fermentation liquor, was supplied into a heating apparatus 3 while the fermentation liquor was maintained in an anaerobic state at a dissolved oxygen concentration of 0.1 mg/lit. The requisite minimal heating times (2 - 42 minutes) were obtained in the same manner as in Example 1, and the fermentation liquor was heated under various heating conditions (temperature, time and pressure) and then cooled to give samples (Samples 4 - 7).
  • As shown in Table 3, it was apparent that the contents of the diacetyl compound in the fermentation liquor were decreased after heating under either set of heating conditions, and that for the substantially the same content of the diacetyl compound in the fermentation liquor before heating, the same effect was obtained in a shorter heating time at a higher heating temperature.
    Figure imgb0003
  • Example 4
  • A fermentation liquor which was obtained by the fermentation of a wort by a beer yeast, Saccharomyces cerevisiae, namely the main fermentation liquor, was supplied into a heating apparatus 3 at various dissolved oxygen concentrations. The requisite minimal heating time (20 minutes) was obtained in the same manner as in Example 1, and the fermentation liquor was subjected to heating treatment without pressurizing at a heating temperature of 70°C for a heating time of 40 minutes and then cooled to give a sample.
  • As shown in Fig. 4, a significant effect was observed such that the contents of the diacetyl compound in the fermentation liquor were decreased at a dissolved oxygen concentration of less than 1 mg/lit., and it was desirable to reduce the dissolved oxygen concentration to 0.1 mg/lit. for obtaining a greater effect.
  • Example 5
  • A fermentation liquor which was obtained by the fermentation of a wort by a beer yeast, Saccharomyces cerevisiae, namely the main fermentation liquor, was supplied into a heating apparatus 3 while the fermentation liquor was maintained in an anaerobic state at a dissolved oxygen concentration of 0.1 mg/lit. The fermentation liquor was subjected to heating treatment for various heating times at three levels of heating temperature (60°C, 70°C and 80°C) and then cooled to give samples.
  • As shown in Fug. 5, it was apparent that for substantially the same diacetyl content in the fermentation liquor before heating, the same effect was obtained in a shorter heating time at a higher heating temperature.
  • INDUSTRIAL APPLICABILITY
  • As it is possible according to the present invention to reduce the content of diacetyl which has come from the main fermentation liquor and gives an unpleasant smell to alcoholic beverages by heating the main fermentation liquor for a short time, the post fermentation conventionally carried out at a low temperature for a long time in order to lower the content of diacetyl can be made unnecessary or simplified. Accordingly, the present invention has a large industrial applicability in view that the present invention can greatly shorten the time for producing alcoholic beverages.

Claims (4)

  1. A process for producing alcoholic beverages comprising a step of heating a fermentation liquor obtained by subjecting an aqueous solution which contains a substrate for a microorganism to the fermentation with proliferation of the microorganism taking place, under such a condition that concentration of the dissolved oxygen in the fermentation liquor is maintained at a level lower than 1 mg/lit., to thereby reduce the quantity in the fermentation liquor of the total of the diacetyl and the precursor thereof below the level before the heating.
  2. A process for producing alcoholic beverages according to claim 1, wherein a first graph illustrating the relationship between (i) the heating temperature and (ii) the rate constant for conversion of the diacetyl precursor into diacetyl and a second graph illustrating the relationship between (iii) said conversion rate constant at a combination of the diacetyl precursor content before heating and an aimed residual diacetyl precursor content after heating and (iv) the requisite heating time for obtaining said objective residual diacetyl precursor content after heating are preliminarily obtained, a rate constant for conversion corresponding to the heating time is obtained from the first graph, the heating time which corresponds to said conversion rate constant and also corresponds to the combination of the diacetyl precursor content before heating and objective aimed residual diacetyl precursor content after heating is obtained from the second graph, and the heating temperature of the fermentation liquor is maintained for at least during the aforementioned heating time so obtained.
  3. A process for producing alcoholic beverages according to claims 1 or 2, wherein the heating temperature is in the range of 40 to 120°C.
  4. A process for producing alcoholic beverages according to any one of claims 1, 2 or 3, wherein the aqueous solution which contains a substrate is wort, and the alcoholic beverage is beer.
EP90907420A 1989-05-15 1990-05-15 Method for preparing alcoholic beverages Revoked EP0424545B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP1121164A JPH02299576A (en) 1989-05-15 1989-05-15 Production of japanese wines
JP121164/89 1989-05-15
PCT/JP1990/000610 WO1990014413A1 (en) 1989-05-15 1990-05-15 Method of producing sake

Publications (3)

Publication Number Publication Date
EP0424545A1 true EP0424545A1 (en) 1991-05-02
EP0424545A4 EP0424545A4 (en) 1992-07-08
EP0424545B1 EP0424545B1 (en) 1997-01-29

Family

ID=14804429

Family Applications (1)

Application Number Title Priority Date Filing Date
EP90907420A Revoked EP0424545B1 (en) 1989-05-15 1990-05-15 Method for preparing alcoholic beverages

Country Status (8)

Country Link
EP (1) EP0424545B1 (en)
JP (1) JPH02299576A (en)
KR (1) KR940005573B1 (en)
CN (1) CN1047529A (en)
AU (1) AU629343B2 (en)
CA (1) CA2033093A1 (en)
DE (1) DE69029831T2 (en)
WO (1) WO1990014413A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6570127B2 (en) 2001-05-03 2003-05-27 Praxair Technology, Inc. Shielding gas mixture for MIG brazing

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4305920B2 (en) * 2004-08-03 2009-07-29 麒麟麦酒株式会社 Fermented malt beverage containing lactic acid bacteria or malt substitute fermented beverage, and method for producing the same

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1445083A (en) * 1972-10-20 1976-08-04 Brewing Patents Ltd Brewing of beer
DD151766A1 (en) * 1980-06-26 1981-11-04 Gerolf Annemueller PROCESSES FOR FEEDING AND MATURING
JPS60214873A (en) * 1984-04-10 1985-10-28 Kirin Brewery Co Ltd Production of liquor

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO9014413A1 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6570127B2 (en) 2001-05-03 2003-05-27 Praxair Technology, Inc. Shielding gas mixture for MIG brazing
US6753502B2 (en) 2001-05-03 2004-06-22 Praxair Technology, Inc. Shielding gas mixture for MIG brazing

Also Published As

Publication number Publication date
CA2033093A1 (en) 1990-11-16
WO1990014413A1 (en) 1990-11-29
EP0424545B1 (en) 1997-01-29
EP0424545A4 (en) 1992-07-08
AU629343B2 (en) 1992-10-01
JPH02299576A (en) 1990-12-11
DE69029831T2 (en) 1997-09-04
DE69029831D1 (en) 1997-03-13
CN1047529A (en) 1990-12-05
AU5566890A (en) 1990-12-18
KR920701413A (en) 1992-08-11
KR940005573B1 (en) 1994-06-21

Similar Documents

Publication Publication Date Title
US4970082A (en) Process for preparing a nonalcoholic (less the 0.5 volume percent alcohol) malt beverage
AU2014276195A1 (en) Fermented malt beverage and production method therefor
EP0160442B1 (en) Production of alcoholic beverages
JP4762546B2 (en) Method for producing fermented beverage
JPS6158573A (en) Production of alcoholic beverage
JP2006262860A (en) Method for producing sparkling liquor
JP2005013142A (en) Soft drink having beer taste and method for producing the same
JPH11178564A (en) Production of sparkling wine
EP0424545A1 (en) Method for preparing alcoholic beverages
EP3196285B1 (en) Method for producing saccharified moromi
JPH04197167A (en) Production of liquors
US3402048A (en) Process for producing beer of the vollbier type
JP4024827B2 (en) Production method of malt alcoholic beverage
JP3836254B2 (en) Happoshu manufacturing method
JP3968183B2 (en) Production method of malt alcoholic beverage
Krauss et al. The influence of different fermentation methods on the formation of lower free fatty acids
CN114540138A (en) Method for producing novel fruity acid beer by double-yeast mixed fermentation of wort
JP6456696B2 (en) Method for improving fermentation characteristics of brewer's yeast in fed-batch culture
CN112210452A (en) Preparation method of secondary fresh-keeping fermented beer
KR20240024627A (en) Wort filtration method with high yield efficiency and preparation method of alcoholic beverages using the same
JP2023064993A (en) Fermentation beer-like sparkling drink, and production method of the same
RU2189388C1 (en) METHOD OF PRODUCTION OF BEER "ARSENALNOYE SVETLOYE No
RU2189389C1 (en) METHOD OF PRODUCTION OF STRONG BEER "ARSENALNOYE KREPKOYE No
JPH057989B2 (en)
RU2190012C1 (en) METHOD OF PRODUCING BEER "ARSENALNOYE TEMNOYE No,4"

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19910205

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB NL

A4 Supplementary search report drawn up and despatched

Effective date: 19920520

AK Designated contracting states

Kind code of ref document: A4

Designated state(s): DE FR GB NL

17Q First examination report despatched

Effective date: 19941012

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: KIRIN BEER KABUSHIKI KAISHA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB NL

ET Fr: translation filed
REF Corresponds to:

Ref document number: 69029831

Country of ref document: DE

Date of ref document: 19970313

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19970506

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19970530

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19970531

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19970729

Year of fee payment: 8

PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

26 Opposition filed

Opponent name: TUCHENHAGEN SKANDINAVIEN A/S

Effective date: 19971029

26 Opposition filed

Opponent name: OY PANIMOLABORATORIO-BRYGGERILABORATORIUM AB

Effective date: 19971028

Opponent name: TUCHENHAGEN SKANDINAVIEN A/S

Effective date: 19971029

NLR1 Nl: opposition has been filed with the epo

Opponent name: OY PANIMOLABORATORIO-BRYGGERILABORATORIUM AB

Opponent name: TUCHENHAGEN SKANDINAVIEN A/S

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980515

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19981201

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19980515

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 19981201

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990302

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

RDAH Patent revoked

Free format text: ORIGINAL CODE: EPIDOS REVO

RDAG Patent revoked

Free format text: ORIGINAL CODE: 0009271

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT REVOKED

27W Patent revoked

Effective date: 19990704